HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glyoxal → 7-[1,2,4]Triazin-3-yl-imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glyoxal | HCID 7860 | — |
| Reactant | HCID 178512584 | HCID 178512584 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-[1,2,4]Triazin-3-yl-imidazo[1,2-a]pyridine | HCID 68984228 | 80% |
Reaction Steps
To half the material from step d (ca. 2.3 mmol) was added glyoxal (40% in water, 1 ml) and ethanol (15 ml) and the mixture heated to 100 deg C. After 1 hour the reaction was allowed to cool and was concentrated in vacuo. Water and dichloromethane was added and the mixture filtered under suction. The organic liquors were discarded and the aqueous layer was basified with 2N sodium hydroxide solution. To this was added dichloromethane and the mixture was again filtered under suction. The dichloromethane layer was separated and concentrated to furnish 289 mg of a yellow solid (80% clean). MS: [M+H]+198
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796244B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-2367ad7f05f946268ed91ae7f1029057 |
| Source note | uspto-grants-2014_08 |